Varaico: Literature-Extracted Genetic Variants

Gene:SOS1
Variant:p.L569V
Back to variants list

SOS1

NM_005633.4:p.L569V

Associated Papers

Inside the Noonan "universe": Literature review on growth, GH/IGF axis and rhGH treatment: Facts and concerns.

Stagi S et al.

Frontiers in Endocrinology, 2022

Germline mutations in candidate predisposition genes in individuals with cutaneous melanoma and at least two independent additional primary cancers.

Pritchard AL et al.

Plos One, 2018

29641532 (PubMed )
Supplement: pone.0194098.s003.xlsx › UK10K_AD

SOS1 mutations in Noonan syndrome: molecular spectrum, structural insights on pathogenic effects, and genotype-phenotype correlations.

Lepri F et al.

Human Mutation, 2011

Tumor spectrum in children with Noonan syndrome and SOS1 or RAF1 mutations.

Denayer E et al.

Genes, Chromosomes & Cancer, 2010

Genome profiling of chronic myelomonocytic leukemia: frequent alterations of RAS and RUNX1 genes.

Gelsi-Boyer V et al.

Bmc Cancer, 2008

Select a paper to view details
UCSC Genome Browser·Imprint·Privacy·Terms·Feedback·Email Updates·

Regarding the variants extracted from papers and shown text snippets from research papers, the following holds: "Some rights reserved. This work permits non-commercial use, distribution and reproduction in any medium, provided the original author and source are credited."